GET TESTED International AB recalls all Chlamy: Test products due to distribution without premarket approval. No specific action steps provided in recall notice.
Distribution without premarket approval/clearance.
GET TESTED International AB has recalled all Chlamydia Test products because they were distributed without proper premarket approval. This recall does not include specific instructions for consumers to stop using or return the product.
The product was distributed without premarket approval, meaning it may not have met safety standards before being sold. This could potentially lead to health risks if the test is not accurate or safe for use.
Anyone who purchased the Chlamydia Test product from the manufacturer. The recall applies to all units produced.
The product is labeled as 'Chlamydia Test' with EAN: 7340221701663 and SKU: A-ICH. All lots of this product are affected.
Look for the EAN code 7340221701663 and SKU A-ICH on the product label.
The recall notice does not provide specific action steps for consumers.
The product was distributed without premarket approval, which may indicate it did not meet safety standards.
The product has EAN: 7340221701663 and SKU: A-ICH. All lots are affected.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0730-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0730-2026 from GET TESTED. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
